# Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products, Division PART 3:: SAFETY AND RESIDUES TESTS

Extent: E+W+S+N.I.

The particulars and documents which shall accompany the application for marketing authorisation pursuant to the second and fourth indents of Article 12(3)(j) shall be submitted in accordance with the requirements below.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/I/part/3 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.